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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82789Generated: October 30, 2026

Sodium hydride → 5-((2,6-Difluoro-4-hydroxyphenethyl)(4H-1,2,4-triazol-4-yl)amino)biphenyl-2-carbonitrile

https://huagongshe.com/reaction/82789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(4-(2-Bromoethyl)-3,5-difluorophenoxy)triisopropylsilaneHCID 68004578—
Reactant5-(4H-1,2,4-triazol-4-ylamino)biphenyl-2-carbonitrileHCID 68227992—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
Product5-((2,6-Difluoro-4-hydroxyphenethyl)(4H-1,2,4-triazol-4-yl)amino)biphenyl-2-carbonitrileHCID 6822855550%

Reaction Steps

NaH (60% dispersion in mineral oil, 0.039 g, 0.98 mmol) was added to a solution of 5-(4H-1,2,4-triazol-4-ylamino)biphenyl-2-carbonitrile (CAB06022) (0.23 g, 0.88 mmol) in DMF (5 mL). After stirring for 30 minutes a solution of PMW04158 (0.38 g, 0.97 mmol) in DMF (3 mL) was added and stirring was continued for 48 h. TBAF (1M in THF, 1.35 mL) was added and after 30 minutes the reaction mixture was poured onto H2O (15 mL) and acidified with 3M aq. AcOH. The product was extracted with EtOAc (0.3×25 ml) and the combined organics were washed with H2O (4×50 ml) and brine (50 mL) then dried (MgSO4) and the solvent was removed in vacuo. The crude product was purified using the Combiflash system (CHCl3/Acetone) to give the title compound (0.18 g, 50%) as a white solid; 1H NMR (270 MHz, DMSO-d6) 2.81 (2H, t, J=7.5, CH2), 4.01 (2H, t, J=7.5, CH2), 6.41-6.51 m, ArH), 6.61 (1H, d, J=2.2, ArH), 7.45-7.56 (5H, m, ArH), 7.83 (1H, d, J=8.8, ArH), 8.93 (2H, s, NCHN), 10.40 (1H, s, OH); HRMS (ESS) calcd. for C13H18F2N5O1 (M++1) 418.1474. found 418.1466; LC/MS (ES+) tr=1.39 min, m/z 418.0 (M++1, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846737B2
Source datasetuspto-grants-2014_09
ORD IDord-c5adf8a4d2d445f8b733557795e1a79d
Source noteuspto-grants-2014_09